The coupling of Thermogravimetry (TG) in conjuction with chemometrics was investigated for the first time to evaluate the capabilities of this novel test to provide the screening of thalassemia in blood samples stored at 4 °C until 15 days. Healthy donors were considered as reference subjects and a typical thermal behaviour as a function of aging was estimated and compared to thermal behaviour of thalassemia subjects. Diagnosis of thalassemia was made at the Day-Hospital Thalassemia of S. Eugenio Hospital through a comprehensive assessment of clinical presentation and hematological and molecular analysis. Despite blood changes with aging, the application of the TGA/Chemometrics test reveal that healthy and thalassemic population may be sign...
β-Thalassemia carrier’s frequency is uneven in different districts in Gujarat (0–9.5%). Surat Raktad...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Introduction: Morbidity and mortality in beta thalassemia are caused by anemia and iron overload. T...
A novel approach based on Thermogravimetric analysis followed by Chemometrics (TGA/Chemometrics) is ...
Thermogravimetry coupled with chemometrics has proved to be a rapid and cost-effective diagnostic to...
Introduction: Hemoglobinopathies are the most common genetic disorder wordlwide and because of migra...
In this study the TGA/Chemometric test was applied for diagnosis of a case of congenital hemolytic a...
In a retrospective study of 36 cases of alpha-thalassaemia trait, 43 cases of beta-thalassaemia trai...
Introduction The standard screening method for alpha thalassaemia is the examination of HbH prepara...
The α and β-thalassaemias (thal) are common genetic disorders of globin chain synthesis where the ca...
The thalassemias can be defined as \u3b1- or \u3b2-thalassemias depending on the defective globin ch...
Thalassemia is an inherited disorder resulting from a mutation or deletion of a gene that causes one...
The current study aims to study some biochemical indicators for thalassemia patients in the Najaf go...
Study DesignThis cross-sectional study was conducted in Palestine among multi-transfused thalassemia...
The current study aims to study some biochemical indicators for thalassemia patients in the Najaf go...
β-Thalassemia carrier’s frequency is uneven in different districts in Gujarat (0–9.5%). Surat Raktad...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Introduction: Morbidity and mortality in beta thalassemia are caused by anemia and iron overload. T...
A novel approach based on Thermogravimetric analysis followed by Chemometrics (TGA/Chemometrics) is ...
Thermogravimetry coupled with chemometrics has proved to be a rapid and cost-effective diagnostic to...
Introduction: Hemoglobinopathies are the most common genetic disorder wordlwide and because of migra...
In this study the TGA/Chemometric test was applied for diagnosis of a case of congenital hemolytic a...
In a retrospective study of 36 cases of alpha-thalassaemia trait, 43 cases of beta-thalassaemia trai...
Introduction The standard screening method for alpha thalassaemia is the examination of HbH prepara...
The α and β-thalassaemias (thal) are common genetic disorders of globin chain synthesis where the ca...
The thalassemias can be defined as \u3b1- or \u3b2-thalassemias depending on the defective globin ch...
Thalassemia is an inherited disorder resulting from a mutation or deletion of a gene that causes one...
The current study aims to study some biochemical indicators for thalassemia patients in the Najaf go...
Study DesignThis cross-sectional study was conducted in Palestine among multi-transfused thalassemia...
The current study aims to study some biochemical indicators for thalassemia patients in the Najaf go...
β-Thalassemia carrier’s frequency is uneven in different districts in Gujarat (0–9.5%). Surat Raktad...
Thalassaemia screening programme has been conducted in Malaysia since 2004. The aim of the programme...
Introduction: Morbidity and mortality in beta thalassemia are caused by anemia and iron overload. T...